Increased IgM levels
Basic details
Preferred term: Increased IgM levels
Alt. terms: Increased levels of IgM | Increased circulating IgM level
HPO term: Increased circulating IgM level
HPO code: HP:0003496
GenIA ID: 23
Last updated on: 2021-12-10 17:55:48
Cross ref. with other ontologies
NCIT: -
MESH: -
EFO: -
OAE: -
SNOMEDCT: -
ICD10: -
Description
An abnormally increased level of immunoglobulin M in blood.
Hierarchical classification
TERM
Increased IgM levels
Reported patients added to GenIA DB
SubjectID | Sex | Fam.ID | Age* | Population | MatchedTerm | Diagnosis | Reference & Pub.codes |
---|---|---|---|---|---|---|---|
101028 | F | 210750 | 42 | German | Increased IgM levels | PMID:34975878 [Fam.F013:P013] | |
101043 | M | 210725![]() |
20 | Caucasian | Increased IgM levels | CTLA4 haploinsufficiency with autoimmune infiltration | PMID:29729943 [Fam.H:II.2(30)]; PMID:34975878 [Fam.F017:P017] |
101104 | F | 211429 | 5 | Increased IgM levels | Activated p110-delta syndrome 1 | PMID:34975878 [Fam.F397:P397] | |
101139 | F | 212090 | 25 | Increased IgM levels | PMID:34975878 [Fam.F399:P399] | ||
101444 | F | 210640 | 35 | Increased IgM levels | PMID:34975878 [Fam.F145:P145] | ||
101501 | F | 212459 | - | British | Increased IgM levels | Activated p110-delta syndrome 1 | PMID:24136356 [Fam.A:II.2(P4)] |
101509 | F | 212459 | - | British | Increased IgM levels | Activated p110-delta syndrome 1 | PMID:24136356 [Fam.A:III.2(P1)] |
101511 | M | 212459 | - | British | Increased IgM levels | Activated p110-delta syndrome 1 | PMID:24136356 [Fam.A:III.3(P2)] |
101512 | M | 212459 | - | British | Increased IgM levels | Activated p110-delta syndrome 1 | PMID:24136356 [Fam.A:III.4(P3)] |
101530 | M | 212460 | - | British | Increased IgM levels | Activated p110-delta syndrome 1 | PMID:24136356 [Fam.B:III.3(P5)] |
101532 | F | 212460 | - | British | Increased IgM levels | Activated p110-delta syndrome 1 | PMID:24136356 [Fam.B:III.5(P6)] |
101534 | M | 212460 | - | British | Increased IgM levels | Activated p110-delta syndrome 1 | PMID:24136356 [Fam.B:IV.1(P11)] |
101541 | M | 212461 | - | Slovenian | Increased IgM levels | Activated p110-delta syndrome 1 | PMID:24136356 [Fam.C:II.1(P8)] |
101546 | F | 212462 | - | Irish | Increased IgM levels | Activated p110-delta syndrome 1 | PMID:24136356 [Fam.D:II.1(P10)] |
101548 | M | 212462 | - | Irish | Increased IgM levels | Activated p110-delta syndrome 1 | PMID:24136356 [Fam.D:III.1(P9)] |
101549 | F | 212463 | - | British | Increased IgM levels | Activated p110-delta syndrome 1 | PMID:24136356 [Fam.E:I.1(P13)] |
101552 | M | 212464 | - | French | Increased IgM levels | Activated p110-delta syndrome 1 | PMID:24136356 [Fam.F:II.1(P14)] |
101560 | M | 212465 | - | French | Increased IgM levels | Activated p110-delta syndrome 1 | PMID:24136356 [Fam.G:II.2(P15)] |
101561 | F | 212465 | - | French | Increased IgM levels | Activated p110-delta syndrome 1 | PMID:24136356 [Fam.G:II.3(P16)] |
101578 | M | 210205![]() |
33 | German | Increased IgM levels | CTLA4 haploinsufficiency with autoimmune infiltration | PMID:25329329 [Fam.A:II.14(A.II.8)]; PMID:29729943 [Fam.A:II.14(A.II.8 (5))]; PMID:27418640 [P8(5)] |
101596 | M | 212618![]() |
4 | Jewish | Increased IgM levels | ARPC1B deficiency | PMID:29127144 [P1(II.1)] |
101687 | F | 212635![]() |
1 | Nepalese | Increased IgM levels | ARPC1B deficiency | PMID:30771411 [P12(II.1)] |
102216 | F | 214916![]() |
3 | Belgian | Hypergammaglobulinaemia | Severe congenital neutropenia 11 | PMID:32325141 [Patient(II.1)] |
102260 | F | 214926![]() |
- | Mexican | Increased IgM levels | ARPC1B deficiency | PMID:32683750 [Fam.case:II.2(sister)]; PMID:36708766 [Fam.A:II.2(P1)] |
102410 | F | 214947![]() |
1 | South Asian | Increased IgM levels | Hyper-IgE recurrent infection syndrome 4B | PMID:28747427 [Fam.A:II.3(P1)] |
102901 | F | 215008![]() |
0 | Brasilian | Hypergammaglobulinaemia | T-cell immunodeficiency, congenital alopecia, and nail dystrophy | PMID:35064468 [patient(II.2)] |
103547 | M | 215157![]() |
11 | Mexican | Increased IgM levels | ARPC1B deficiency | PMID:36708766 [Fam.D:II.4(P6)] |
104001 | F | 215322![]() |
- | North American | Increased IgM levels | Infantile-Onset Multisystem Autoimmune Disease 1 | PMID:25359994 [P5]; PMID:32392079 [P3]; PMID:30092289 [P15]; PMID:35677041 [Pt3]; PMID:33651637 [Patient 1] |
104540 | M | 215549![]() |
-,- | North African | Hypergammaglobulinaemia,Increased IgM levels | X-linked multisystem autoinflammatory disease with immune dysregulation | PMID:36952639 [Fam.F:II.1(Patient F)] |
104554 | M | 215551![]() |
3 | Pakistani | Increased IgM levels | Autoinflammation, panniculitis, and dermatosis syndrome | PMID:27523608 [Fam.1:V.2(V:2)]; PMID:27559085 [Fam.1:V.2(P1)]; PMID:35587511 [Fam.G:II.2(4)]; PMID:34797715 [P1]; PMID:38914362 [Fam.A:V.2(023)] |
104568 | F | 215551![]() |
0 | Pakistani | Increased IgM levels | Autoinflammation, panniculitis, and dermatosis syndrome | PMID:27523608 [Fam.1:IV.3(IV:3)]; PMID:32231246 [IV:3(IV.3)]; PMID:27559085 [Fam.1:IV.1(P4)]; PMID:38914362 [Fam.A:V.6(027)] |
104846 | F | 215580 | 0 | Egyptian | Increased IgM levels | Omenn syndrome 2 | PMID:30307608 [1] |
105045 | M | 215631![]() |
24 | Caucasian | Increased IgM levels | CTLA4 haploinsufficiency with autoimmune infiltration | PMID:27379089 [P10] |
105093 | F | 215639![]() |
19 | Israeli | Increased IgM levels | NFKB1 insufficiency | PMID:32278790 [Fam.AA:II.2(II.2)]; PMID:29403474 [Patient 2 (8)]; PMID:27365489 [Fam.2:II.2(Pat.2)]; PMID:150198 [Fam.AF:II.2(127)] |
105350 | M | 215712 | 2 | Omani | Hypergammaglobulinaemia | Immunodeficiency, common variable, 8 | PMID:28690850 [P1] |
105481 | M | 215777![]() |
- | Haitian/Hispanic | Increased IgM levels | Activated p110-delta syndrome 1 | PMID:24165795 [Fam.A:II.1(A.1)] |
105482 | F | 215778![]() |
- | Caucasian | Increased IgM levels | Activated p110-delta syndrome 1 | PMID:24165795 [Fam.B:I.2(I.2)] |
105484 | F | 215778![]() |
- | Caucasian | Increased IgM levels | Activated p110-delta syndrome 1 | PMID:24165795 [Fam.B:III.1(B.III.1)] |
105487 | F | 215780![]() |
- | Afro-American | Increased IgM levels | Activated p110-delta syndrome 1 | PMID:24165795 [Fam.G:II.1(G.1)] |
105537 | M | 215793 | - | Increased IgM levels | Activated p110-delta syndrome 1 | PMID:24698326 [P1] | |
105587 | F | 215820 | - | Caucasian | Increased IgM levels | Activated p110-delta syndrome 1 | PMID:24610295 [Fam.1:II.1(F1P1)] |
105591 | F | 215821 | - | Caucasian | Increased IgM levels | Activated p110-delta syndrome 1 | PMID:24610295 [Fam.2:II.1(F2P2)] |
105607 | F | 215821 | - | Caucasian | Increased IgM levels | PMID:24610295 [Fam.2:II.3] | |
105609 | M | 215821 | - | Caucasian | Increased IgM levels | Activated p110-delta syndrome 1 | PMID:24610295 [Fam.2:III.1(F2P3)] |
105617 | F | 215822 | - | Caucasian | Increased IgM levels | PMID:25352054 [Fam.1:I.1(I.1)] | |
105626 | M | 215822 | - | Caucasian | Increased IgM levels | Activated p110-delta syndrome 1 | PMID:25352054 [Fam.1:III.1(P3)] |
105627 | F | 215822 | 3 | Caucasian | Increased IgM levels | Activated p110-delta syndrome 1 | PMID:25352054 [Fam.1:III.2(P4)] |
105628 | F | 215822 | - | Caucasian | Increased IgM levels | Activated p110-delta syndrome 1 | PMID:25352054 [Fam.1:III.3(P5)] |
105635 | F | 215829 | - | Caucasian | Increased IgM levels | Activated p110-delta syndrome 1 | PMID:26371693 [1] |
105657 | F | 215835 | - | Increased IgM levels | Activated p110-delta syndrome 1 | PMID:27379089 [11] | |
106352 | M | 215998![]() |
3 | Increased IgM levels | Activated p110-d syndrome 2 | PMID:34922003 [Fam.B:II.1(B1)] | |
106463 | F | 216023![]() |
- | Japanese | Hypergammaglobulinaemia | NFKB1 insufficiency | PMID:150198 [Fam.FX:II.3(779)]; PMID:38514645 [Fam.1:II.3(proband)] |
106642 | F | 216097 | 2 | European | Hypergammaglobulinaemia | CTLA4 haploinsufficiency with autoimmune infiltration | PMID:31396201 [Fam.:II.1(P1)] |
106888 | M | 216182![]() |
10 | Caucasian | Hypergammaglobulinaemia | Adenosine deaminase 2 deficiency | PMID:28830446 [P1(II.1)] |
106889 | M | 216182![]() |
4 | Caucasian | Hypergammaglobulinaemia | Adenosine deaminase 2 deficiency | PMID:28830446 [Fam.P1:II.2(P2)] |
106932 | M | 216188![]() |
5 | Jewish | Hypergammaglobulinaemia | Adenosine deaminase 2 deficiency | PMID:25075848 [patient]; PMID:30139808 [Fam.1:II.5(P)] |
107176 | M | 216369 | - | Hypergammaglobulinaemia | T-cell LGL leukemia 1 | PMID:26419508 [Patient 1] | |
107226 | M | 216382 | 13 | North American | Increased IgM levels | Infantile-Onset Multisystem Autoimmune Disease 1 | PMID:35677041 [Pt6]; PMID:33651637 [Patient 2]; PMID:28349047 [Case] |
*Age: age reported at the first known time of manifestation; PMID: PubMed ID; GRID: GenIA reference ID (ref. not in PubMed).